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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does RIFAXIMIN Cause Condition aggravated? 420 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 420 reports of Condition aggravated have been filed in association with RIFAXIMIN (XIFAXAN). This represents 3.0% of all adverse event reports for RIFAXIMIN.

420
Reports of Condition aggravated with RIFAXIMIN
3.0%
of all RIFAXIMIN reports
61
Deaths
205
Hospitalizations

How Dangerous Is Condition aggravated From RIFAXIMIN?

Of the 420 reports, 61 (14.5%) resulted in death, 205 (48.8%) required hospitalization, and 3 (0.7%) were considered life-threatening.

Is Condition aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for RIFAXIMIN. However, 420 reports have been filed with the FAERS database.

What Other Side Effects Does RIFAXIMIN Cause?

Death (3,687) Hospitalisation (1,605) Therapy interrupted (875) Off label use (802) Diarrhoea (709) Ammonia increased (676) Inability to afford medication (672) Insurance issue (577) Confusional state (530) Hepatic cirrhosis (480)

What Other Drugs Cause Condition aggravated?

TOFACITINIB (16,925) INFLIXIMAB (16,616) DUPILUMAB (16,459) ETANERCEPT (15,897) METHOTREXATE (14,938) ADALIMUMAB (13,527) PREDNISONE (10,751) INFLIXIMAB-DYYB (10,275) HYDROXYCHLOROQUINE (8,848) RITUXIMAB (8,627)

Which RIFAXIMIN Alternatives Have Lower Condition aggravated Risk?

RIFAXIMIN vs RILMENIDINE RIFAXIMIN vs RILONACEPT RIFAXIMIN vs RILPIVIRINE RIFAXIMIN vs RILUZOLE RIFAXIMIN vs RIMABOTULINUMTOXINB

Related Pages

RIFAXIMIN Full Profile All Condition aggravated Reports All Drugs Causing Condition aggravated RIFAXIMIN Demographics